Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.17 (C)

Chromosome 2:46302122 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58865021

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2506 sample genotypes.

Variant displays